Statistical Programmer

Principal SAS Programmer - Hybrid Contract - Remote (2 days/week onsite - Philadelphia)

Exclusively partnered with a lead consultancy looking to expand the team with a Principal SAS Programmer. In this role you'll be supporting regulatory submissions/clinical trial design and driving forward our exciting early phase pipeline projects.

Responsibilities:

Lead statistical programming efforts for regulatory submissions

Collaborate closely with cross-functional teams to ensure timely and accurate deliverables

Utilize your expertise in SAS programming to develop and maintain analysis algorithms and processes

Provide guidance and mentorship to junior team members

Requirements:

Bachelor's or Master's degree in a relevant field

Minimum of 7 years of experience in statistical programming within the Biotech/Pharma industry

Proven track record of direct submissions experience (5+ years)

Strong proficiency in SAS programming

Expertise in Mixed Modeling and Efficacy Programming

Excellent communication and problem-solving skills

Interviews are happening this week, so reach out asap!

#PrincipalSASProgrammer #BiomedicalStatistics #HybridWorkModel